BR112014018528A8 - PYRIDO [2,3] PYRIMIDINE 2-AMINO, 6-PHENYL SUBSTITUTED DERIVATIVES USEFUL AS RAF KINASE INHIBITORS - Google Patents

PYRIDO [2,3] PYRIMIDINE 2-AMINO, 6-PHENYL SUBSTITUTED DERIVATIVES USEFUL AS RAF KINASE INHIBITORS

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Publication number
BR112014018528A8
BR112014018528A8 BR112014018528A BR112014018528A BR112014018528A8 BR 112014018528 A8 BR112014018528 A8 BR 112014018528A8 BR 112014018528 A BR112014018528 A BR 112014018528A BR 112014018528 A BR112014018528 A BR 112014018528A BR 112014018528 A8 BR112014018528 A8 BR 112014018528A8
Authority
BR
Brazil
Prior art keywords
pyrido
pyrimidine
amino
kinase inhibitors
phenyl substituted
Prior art date
Application number
BR112014018528A
Other languages
Portuguese (pt)
Other versions
BR112014018528A2 (en
Inventor
Carl Allgeier Matthew
L Flynn Daniel
D Kaufman Michael
J Patel Phenil
D Wolfangel Craig
Original Assignee
Lilly Co Eli
Deciphera Pharmaceuticals Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47884613&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BR112014018528(A8) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli, Deciphera Pharmaceuticals Llc filed Critical Lilly Co Eli
Publication of BR112014018528A2 publication Critical patent/BR112014018528A2/pt
Publication of BR112014018528A8 publication Critical patent/BR112014018528A8/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)

Abstract

DERIVADOS DE PIRIDO [2,3] PIRIMIDINA 2-AMINO, 6-FENIL SUBSTITUÍDOS ÚTEIS COMO INIBIDORES DE RAF QUINASE. A presente invenção refere-se ao composto 1-(3,3-dimetilbutil)-3-(2-fluor-4-metil-5-(7-metil-2-(metilamino)pirido[2,3-d]pirimidin-6-il)fenil) ureia ou um sal farmaceuticamente aceitável desse que inibe Raf e, portanto, pode ser útil no tratamento do câncer.PYRIDO [2,3] PYRIMIDINE 2-AMINO, 6-PHENYL SUBSTITUTED DERIVATIVES USEFUL AS RAF KINASE INHIBITORS. The present invention relates to the compound 1-(3,3-dimethylbutyl)-3-(2-fluoro-4-methyl-5-(7-methyl-2-(methylamino)pyrido[2,3-d]pyrimidin -6-yl)phenyl)urea or a pharmaceutically acceptable salt thereof which inhibits Raf and therefore may be useful in the treatment of cancer.

BR112014018528A 2012-03-07 2013-03-05 PYRIDO [2,3] PYRIMIDINE 2-AMINO, 6-PHENYL SUBSTITUTED DERIVATIVES USEFUL AS RAF KINASE INHIBITORS BR112014018528A8 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261607702P 2012-03-07 2012-03-07
PCT/US2013/029084 WO2013134243A1 (en) 2012-03-07 2013-03-05 2-amino, 6-phenyl substituted pyrido [2, 3 - d] pyrimidine derivatives useful as raf kinase inhibitors

Publications (2)

Publication Number Publication Date
BR112014018528A2 BR112014018528A2 (en) 2017-06-20
BR112014018528A8 true BR112014018528A8 (en) 2017-07-11

Family

ID=47884613

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112014018528A BR112014018528A8 (en) 2012-03-07 2013-03-05 PYRIDO [2,3] PYRIMIDINE 2-AMINO, 6-PHENYL SUBSTITUTED DERIVATIVES USEFUL AS RAF KINASE INHIBITORS

Country Status (39)

Country Link
US (2) US8741911B2 (en)
EP (1) EP2850082B1 (en)
JP (1) JP2015509536A (en)
KR (1) KR20140129087A (en)
CN (1) CN104302646B (en)
AP (1) AP2014007899A0 (en)
AR (1) AR090151A1 (en)
AU (1) AU2013230146B2 (en)
BR (1) BR112014018528A8 (en)
CA (1) CA2863673A1 (en)
CL (1) CL2014002220A1 (en)
CO (1) CO7010837A2 (en)
CR (1) CR20140378A (en)
CY (1) CY1117846T1 (en)
DK (1) DK2850082T3 (en)
DO (1) DOP2014000200A (en)
EA (1) EA024824B1 (en)
EC (1) ECSP14017584A (en)
ES (1) ES2584387T3 (en)
HK (1) HK1202541A1 (en)
HR (1) HRP20160654T1 (en)
HU (1) HUE028095T2 (en)
IL (1) IL234052A (en)
IN (1) IN2014MN01575A (en)
LT (1) LT2850082T (en)
MA (1) MA37316B1 (en)
ME (1) ME02423B (en)
MX (1) MX2014010701A (en)
NZ (1) NZ627454A (en)
PE (1) PE20142338A1 (en)
PH (1) PH12014501986A1 (en)
PT (1) PT2850082T (en)
RS (1) RS54840B1 (en)
SG (1) SG11201404969YA (en)
SI (1) SI2850082T1 (en)
TN (1) TN2014000375A1 (en)
TW (1) TW201348233A (en)
UA (1) UA112340C2 (en)
WO (2) WO2013134243A1 (en)

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AR090151A1 (en) * 2012-03-07 2014-10-22 Lilly Co Eli RAF INHIBITING COMPOUNDS
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TWI704151B (en) 2014-12-22 2020-09-11 美商美國禮來大藥廠 Erk inhibitors
AU2017279046B2 (en) * 2016-06-10 2020-07-02 Novartis Ag Therapeutic uses of a c-Raf inhibitor
EP3878850A1 (en) 2016-12-22 2021-09-15 Boehringer Ingelheim International GmbH Novel benzylamino substituted quinazolines and derivatives as sos1 inhibitors
CA3060147A1 (en) * 2017-04-28 2018-11-01 Quartz Therapeutics, Inc. Raf-degrading conjugate compounds
CR20210307A (en) 2017-12-21 2021-07-27 Boehringer Ingelheim Int Novel benzylamino substituted pyridopyrimidinones and derivatives as sos1 inhibitors
JP7161849B2 (en) * 2018-01-24 2022-10-27 株式会社クラレ Method for producing primary amine
CN111818915B (en) 2018-01-31 2024-05-24 德西费拉制药有限责任公司 Combination therapy for the treatment of gastrointestinal stromal tumors
WO2020055760A1 (en) 2018-09-10 2020-03-19 Mirati Therapeutics, Inc. Combination therapies
EP3902547B1 (en) 2018-12-28 2023-09-20 Deciphera Pharmaceuticals, LLC Csf1r inhibitors for use in treating cancer
WO2020163268A1 (en) 2019-02-06 2020-08-13 Eli Lilly And Company 1-((2-(2,2,2-trifluoroethoxy)pyridin-4-yl)methyl)urea derivatives as kcnq potentiators
WO2020227020A1 (en) 2019-05-03 2020-11-12 Kinnate Biopharma Inc. Inhibitors of raf kinases
US11518758B2 (en) 2019-05-10 2022-12-06 Deciphera Pharmaceuticals, Llc Heteroarylaminopyrimidine amide autophagy inhibitors and methods of use thereof
FI3966207T3 (en) 2019-05-10 2023-11-30 Deciphera Pharmaceuticals Llc Phenylaminopyrimidine amide autophagy inhibitors and methods of use thereof
KR20220024605A (en) 2019-06-17 2022-03-03 데시페라 파마슈티칼스, 엘엘씨. Aminopyrimidine amide autophagy inhibitors and methods of use thereof
TW202122082A (en) 2019-08-12 2021-06-16 美商迪賽孚爾製藥有限公司 Methods of treating gastrointestinal stromal tumors
KR20220045189A (en) 2019-08-12 2022-04-12 데시페라 파마슈티칼스, 엘엘씨. How to treat gastrointestinal stromal tumors
JP2023509628A (en) 2019-12-30 2023-03-09 デシフェラ・ファーマシューティカルズ,エルエルシー 1-(4-bromo-5-(1-ethyl-7-(methylamino)-2-oxo-1,2-dihydro-1,6-naphthyridin-3-yl)-2-fluorophenyl)-3- Composition of phenylurea
EP4327827A3 (en) 2019-12-30 2024-05-29 Deciphera Pharmaceuticals, LLC Amorphous kinase inhibitor formulations and methods of use thereof
US11945812B2 (en) 2020-06-02 2024-04-02 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
US11407737B2 (en) 2020-09-18 2022-08-09 Kinnate Biopharma Inc. Inhibitors of RAF kinases
US11377431B2 (en) 2020-10-12 2022-07-05 Kinnate Biopharma Inc. Inhibitors of RAF kinases
JP2023550591A (en) 2020-11-02 2023-12-04 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Substituted 1H-pyrazolo[4,3-c] and derivatives as EGFR inhibitors
EP4247795A1 (en) 2020-11-18 2023-09-27 Deciphera Pharmaceuticals, LLC Gcn2 and perk kinase inhibitors and methods of use thereof
CN117396472A (en) 2020-12-22 2024-01-12 上海齐鲁锐格医药研发有限公司 SOS1 inhibitors and uses thereof
CN117561057A (en) 2021-04-23 2024-02-13 金耐特生物制药公司 Treatment of cancer with RAF inhibitors
US20220388986A1 (en) 2021-04-29 2022-12-08 Boehringer Ingelheim International Gmbh Heterocyclic compounds capable of activating sting
AU2022402390A1 (en) 2021-12-01 2024-05-30 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
TW202340208A (en) 2021-12-01 2023-10-16 德商百靈佳殷格翰國際股份有限公司 Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023099592A1 (en) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023099608A1 (en) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
TW202340209A (en) 2021-12-01 2023-10-16 德商百靈佳殷格翰國際股份有限公司 Annulated 2-amino-3-cyano thiophenes and derivatives for the treatment of cancer
WO2023099620A1 (en) 2021-12-01 2023-06-08 Boehringer Ingelheim International Gmbh Kras degrading compounds comprising annulated 2-amino-3-cyano thiophenes
CA3240192A1 (en) 2021-12-09 2023-06-15 Daniel L. Flynn Raf kinase inhibitors and methods of use thereof
WO2023118250A1 (en) 2021-12-23 2023-06-29 Boehringer Ingelheim International Gmbh 8-aza quinazolines as brain-penetrant sos1-inhibitors
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US7495104B2 (en) * 2001-10-17 2009-02-24 Kirin Beer Kabushiki Kaisha Quinoline or quinazoline derivatives inhibiting auto-phosphorylation of fibroblast growth factor receptors
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AR090151A1 (en) * 2012-03-07 2014-10-22 Lilly Co Eli RAF INHIBITING COMPOUNDS

Also Published As

Publication number Publication date
AU2013230146B2 (en) 2015-09-10
CN104302646A (en) 2015-01-21
HK1202541A1 (en) 2015-10-02
EP2850082A1 (en) 2015-03-25
LT2850082T (en) 2016-09-12
CO7010837A2 (en) 2014-07-31
PH12014501986B1 (en) 2014-11-24
MA37316A1 (en) 2016-06-30
IN2014MN01575A (en) 2015-05-08
SG11201404969YA (en) 2014-10-30
BR112014018528A2 (en) 2017-06-20
TN2014000375A1 (en) 2015-12-21
CR20140378A (en) 2014-11-27
CL2014002220A1 (en) 2015-06-05
US8741911B2 (en) 2014-06-03
AR090151A1 (en) 2014-10-22
KR20140129087A (en) 2014-11-06
HRP20160654T1 (en) 2016-07-01
HUE028095T2 (en) 2016-11-28
MA37316B1 (en) 2017-03-31
PT2850082T (en) 2016-07-15
WO2013134252A1 (en) 2013-09-12
AP2014007899A0 (en) 2014-08-31
DK2850082T3 (en) 2016-08-15
MX2014010701A (en) 2015-03-10
JP2015509536A (en) 2015-03-30
EA024824B1 (en) 2016-10-31
EA201491456A1 (en) 2014-12-30
NZ627454A (en) 2016-09-30
US9334267B2 (en) 2016-05-10
US20130252977A1 (en) 2013-09-26
CN104302646B (en) 2016-05-04
AU2013230146A1 (en) 2014-08-14
US20150119392A1 (en) 2015-04-30
WO2013134243A1 (en) 2013-09-12
ME02423B (en) 2016-09-20
UA112340C2 (en) 2016-08-25
PE20142338A1 (en) 2015-01-10
ECSP14017584A (en) 2016-01-29
ES2584387T3 (en) 2016-09-27
CY1117846T1 (en) 2017-05-17
IL234052A (en) 2016-05-31
EP2850082B1 (en) 2016-05-18
SI2850082T1 (en) 2016-07-29
DOP2014000200A (en) 2014-10-15
PH12014501986A1 (en) 2014-11-24
RS54840B1 (en) 2016-10-31
CA2863673A1 (en) 2013-09-12
TW201348233A (en) 2013-12-01

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Legal Events

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B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]
B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]